Evidence map›Paper›PMID 35764908›Full record

ReviewMolecular imaging and biology2023

Highlighting the Undetectable - Fluorescence Molecular Imaging in Gastrointestinal Endoscopy.

Judith A Stibbe, Petra Hoogland, Friso B Achterberg, Derek R Holman, Raoul S Sojwal, Jacobus Burggraaf, Alexander L Vahrmeijer, Wouter B Nagengast, Stephan Rogalla

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular imaging and biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.0field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Judith A Stibbe *Department of Surgery, Leiden University Medical Center, Leiden University, Leiden, The Netherlands.
Petra Hoogland *Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Friso B AchterbergDepartment of Surgery, Leiden University Medical Center, Leiden University, Leiden, The Netherlands.
Derek R HolmanDepartment of Medicine, Division of Gastroenterology, Stanford University School of Medicine, Stanford, CA, USA.
Raoul S SojwalDepartment of Medicine, Division of Gastroenterology, Stanford University School of Medicine, Stanford, CA, USA.
Jacobus BurggraafDepartment of Surgery, Leiden University Medical Center, Leiden University, Leiden, The Netherlands.
Alexander L VahrmeijerDepartment of Surgery, Leiden University Medical Center, Leiden University, Leiden, The Netherlands.
Wouter B NagengastDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. w.b.nagengast@umcg.nl.
Stephan RogallaDepartment of Medicine, Division of Gastroenterology, Stanford University School of Medicine, Stanford, CA, USA. srogalla@stanford.edu.ORCID 0000-0002-1311-2672
Leiden University Medical Center · NLStanford University · USUniversity Medical Center Groningen · NLStanford Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flexible high-definition white-light endoscopy is the current gold standard in screening for cancer and its precursor lesions in the gastrointestinal tract. However, miss rates are high, especially in populations at high risk for developing gastrointestinal cancer (e.g., inflammatory bowel disease, Lynch syndrome, or Barrett's esophagus) where lesions tend to be flat and subtle. Fluorescence molecular endoscopy (FME) enables intraluminal visualization of (pre)malignant lesions based on specific biomolecular features rather than morphology by using fluorescently labeled molecular probes that bind to specific molecular targets. This strategy has the potential to serve as a valuable tool for the clinician to improve endoscopic lesion detection and real-time clinical decision-making. This narrative review presents an overview of recent advances in FME, focusing on probe development, techniques, and clinical evidence. Future perspectives will also be addressed, such as the use of FME in patient stratification for targeted therapies and potential alliances with artificial intelligence. KEY MESSAGES: • Fluorescence molecular endoscopy is a relatively new technology that enables safe and real-time endoscopic lesion visualization based on specific molecular features rather than on morphology, thereby adding a layer of information to endoscopy, like in PET-CT imaging. • Recently the transition from preclinical to clinical studies has been made, with promising results regarding enhancing detection of flat and subtle lesions in the colon and esophagus. However, clinical evidence needs to be strengthened by larger patient studies with stratified study designs. • In the future fluorescence molecular endoscopy could serve as a valuable tool in clinical workflows to improve detection in high-risk populations like patients with Barrett's esophagus, Lynch syndrome, and inflammatory bowel syndrome, where flat and subtle lesions tend to be malignant up to five times more often. • Fluorescence molecular endoscopy has the potential to assess therapy responsiveness in vivo for targeted therapies, thereby playing a role in personalizing medicine. • To further reduce high miss rates due to human and technical factors, joint application of artificial intelligence and fluorescence molecular endoscopy are likely to generate added value.

Indexed as

Barrett EsophagusColorectal Neoplasms, Hereditary NonpolyposisArtificial IntelligenceEndoscopyEndoscopy, GastrointestinalHumansMolecular ImagingPositron Emission Tomography Computed TomographyArtificial intelligenceCancerEarly detectionFluorescenceFluorescence molecular endoscopyGastrointestinal endoscopyInflammationMolecular imagingNear-infrared fluorescenceOptical imagingPersonalized medicineTargeted biopsy

Identifiers

PMID35764908
PMCPMC9971088
OpenAlexW4283642497

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.